# K031605: Intelijet Fluid Management System Hermes-Ready

- Pathway: 510(k) (Special)
- Applicant: Smith & Nephew, Inc.
- Decided: Jun 18, 2003 after 27 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Smith & Nephew IntelliJET Fluid Management System: named in the summary without a submission number

## Most influential descendants
- K051326: Smith & Nephew 25 Fluid Management System (2005), 1 descendant of its own
- K171794: Smith & Nephew 25 Fluid Management System (2017), 0 descendants of its own

## Indications for use
The Smith & Nephew IntelliJET Fluid Management System (FMS) is indicated for use during arthroscopic joint surgery to regulate flow of irrigation fluids through the joint to maintain intra-articular pressure for uniform distention and clear visualization of the surgical site.

Source page: https://510kreport.com/device/K031605
Methodology: https://510kreport.com/methodology